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Cystic fibrosis as a disease of misprocessing of the cystic fibrosis transmembrane conductance regulator glycoprotein.囊性纤维化是一种囊性纤维化跨膜传导调节蛋白糖蛋白加工错误的疾病。
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本文引用的文献

1
[Congenital factor V deficiency (parahemophilia) with true hemophilia in two brothers].[两兄弟患先天性因子V缺乏症（副血友病）合并真性血友病]
Bibl Paediatr. 1954;58:575-88.
2
Cystic fibrosis as a disease of misprocessing of the cystic fibrosis transmembrane conductance regulator glycoprotein.囊性纤维化是一种囊性纤维化跨膜传导调节蛋白糖蛋白加工错误的疾病。
Am J Hum Genet. 1999 Jun;64(6):1499-504. doi: 10.1086/302429.
3
ERGIC-53 gene structure and mutation analysis in 19 combined factors V and VIII deficiency families.19个联合因子V和VIII缺乏症家族中的ERGIC-53基因结构与突变分析
Blood. 1999 Apr 1;93(7):2261-6.
4
Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiency.对35个伴有联合因子V - 因子VIII缺乏症家庭的ERGIC - 53基因进行分子分析。
Blood. 1999 Apr 1;93(7):2253-60.
5
COPII and selective export from the endoplasmic reticulum.COPII与内质网的选择性输出
Biochim Biophys Acta. 1998 Aug 14;1404(1-2):67-76. doi: 10.1016/s0167-4889(98)00047-0.
6
COPI in ER/Golgi and intra-Golgi transport: do yeast COPI mutants point the way?内质网/高尔基体中的 COPI 与高尔基体内部运输：酵母 COPI 突变体能否指明方向？
Biochim Biophys Acta. 1998 Aug 14;1404(1-2):33-51. doi: 10.1016/s0167-4889(98)00045-7.
7
Getting into the Golgi.进入高尔基体。
Trends Cell Biol. 1998 Jan;8(1):21-5. doi: 10.1016/s0962-8924(97)01184-7.
8
Nucleation of COPII vesicular coat complex by endoplasmic reticulum to Golgi vesicle SNAREs.内质网到高尔基体囊泡SNARE蛋白介导的COPII囊泡衣被复合体的成核作用。
Science. 1998 Jul 31;281(5377):698-700. doi: 10.1126/science.281.5377.698.
9
Selective transport of cargo between the endoplasmic reticulum and Golgi compartments.内质网与高尔基体区室之间货物的选择性运输。
Histochem Cell Biol. 1998 May-Jun;109(5-6):463-75. doi: 10.1007/s004180050248.
10
Mistargeting of the lectin ERGIC-53 to the endoplasmic reticulum of HeLa cells impairs the secretion of a lysosomal enzyme.凝集素ERGIC-53错定位于HeLa细胞的内质网会损害溶酶体酶的分泌。
J Cell Biol. 1998 Jul 27;142(2):377-89. doi: 10.1083/jcb.142.2.377.

From the ER to the golgi: insights from the study of combined factors V and VIII deficiency.

作者信息

Nichols W C, Ginsburg D

机构信息

Division of Human Genetics, Children's Hospital Medical Center, Cincinnati, OH 45229, USA.

出版信息

Am J Hum Genet. 1999 Jun;64(6):1493-8. doi: 10.1086/302433.

DOI:10.1086/302433
PMID:10330336
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1377892/
Abstract
摘要